Suppr超能文献

丹特病中的维生素A反应性夜盲症。

Vitamin A responsive night blindness in Dent's disease.

作者信息

Sethi Sidharth Kumar, Ludwig Michael, Kabra Madhulika, Hari Pankaj, Bagga Arvind

机构信息

Department of Pediatrics, Division of Pediatric Nephrology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, India.

出版信息

Pediatr Nephrol. 2009 Sep;24(9):1765-70. doi: 10.1007/s00467-009-1198-6. Epub 2009 May 15.

Abstract

Dent's disease is an X-linked renal tubular disorder characterized by low molecular weight proteinuria, hypercalciuria and nephrocalcinosis or nephrolithiasis. The disease is caused by mutations in a renal chloride channel gene, CLCN5. We report on three boys, of Indian origin, with Dent's disease that presented at an early age (1-4 years), with polyuria, polydipsia, salt craving, recurrent vitamin A-responsive night blindness, hypophosphataemic rickets, hypercalciuria and low molecular weight proteinuria. All these patients were found to have novel mutations in the CLCN5 gene.

摘要

登特氏病是一种X连锁肾小管疾病,其特征为低分子量蛋白尿、高钙尿症以及肾钙质沉着或肾结石。该疾病由肾氯通道基因CLCN5的突变引起。我们报告了三名印度裔男孩,他们患有登特氏病,发病年龄较早(1至4岁),表现为多尿、烦渴、嗜盐、复发性维生素A反应性夜盲、低磷血症性佝偻病、高钙尿症和低分子量蛋白尿。所有这些患者均被发现CLCN5基因存在新的突变。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验